CR9244A - AMINO-IMIDAZOLONES FOR THE INHIBITION OF ß-SECRETASA - Google Patents
AMINO-IMIDAZOLONES FOR THE INHIBITION OF ß-SECRETASAInfo
- Publication number
- CR9244A CR9244A CR9244A CR9244A CR9244A CR 9244 A CR9244 A CR 9244A CR 9244 A CR9244 A CR 9244A CR 9244 A CR9244 A CR 9244A CR 9244 A CR9244 A CR 9244A
- Authority
- CR
- Costa Rica
- Prior art keywords
- secretasa
- imidazolones
- inhibition
- amino
- aminoimidazolone
- Prior art date
Links
- 230000005764 inhibitory process Effects 0.000 title 1
- 208000037259 Amyloid Plaque Diseases 0.000 abstract 1
- 102100021257 Beta-secretase 1 Human genes 0.000 abstract 1
- 101000894895 Homo sapiens Beta-secretase 1 Proteins 0.000 abstract 1
- -1 aminoimidazolone compound Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
La presente invencion suministra un compuesto de aminoimidazolona de formula I. Tambien se suministran composiciones y metodos para el uso de estos para inhibir B-secretasa (BACE) y tratar depositos B-amiloides y ovillos neurofibrilares.The present invention provides an aminoimidazolone compound of formula I. Compositions and methods for the use of these are also provided to inhibit B-secretase (BACE) and treat B-amyloid deposits and neurofibrillary clews.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US64380505P | 2005-01-14 | 2005-01-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CR9244A true CR9244A (en) | 2007-09-07 |
Family
ID=36581776
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CR9244A CR9244A (en) | 2005-01-14 | 2007-07-12 | AMINO-IMIDAZOLONES FOR THE INHIBITION OF ß-SECRETASA |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US7563796B2 (en) |
| EP (2) | EP2264036A1 (en) |
| JP (1) | JP2008526966A (en) |
| KR (1) | KR20070095948A (en) |
| CN (1) | CN101103034A (en) |
| AR (1) | AR052458A1 (en) |
| AU (1) | AU2006205127A1 (en) |
| BR (1) | BRPI0606690A2 (en) |
| CA (1) | CA2593515A1 (en) |
| CR (1) | CR9244A (en) |
| GT (1) | GT200600009A (en) |
| IL (1) | IL183938A0 (en) |
| MX (1) | MX2007008555A (en) |
| NO (1) | NO20073099L (en) |
| PA (1) | PA8660001A1 (en) |
| PE (1) | PE20060842A1 (en) |
| RU (1) | RU2007126570A (en) |
| TW (1) | TW200637866A (en) |
| WO (1) | WO2006076284A2 (en) |
| ZA (1) | ZA200705783B (en) |
Families Citing this family (66)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7763609B2 (en) | 2003-12-15 | 2010-07-27 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| US7592348B2 (en) | 2003-12-15 | 2009-09-22 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| US7700603B2 (en) | 2003-12-15 | 2010-04-20 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| ATE444962T1 (en) * | 2004-06-16 | 2009-10-15 | Wyeth Corp | AMINO-5,5-DIPHENYLIMIDAZOLONE DERIVATIVES FOR BETA SECRETASE INHIBITION |
| JP2008503460A (en) * | 2004-06-16 | 2008-02-07 | ワイス | Diphenylimidazopyrimidine and imidazolamine as inhibitors of β-secretase |
| BRPI0607094A2 (en) * | 2005-02-01 | 2009-08-04 | Wyeth Corp | compound of the formula i; use of the compound for the treatment of a disease or disorder associated with excessive baby activity in a patient who needs it; use of the compound to modulate the bace activity; and pharmaceutical composition |
| CN101146769A (en) | 2005-02-14 | 2008-03-19 | 惠氏公司 | Azolylacylguanidines as β-secretase inhibitors |
| SG162790A1 (en) | 2005-06-14 | 2010-07-29 | Schering Corp | Aspartyl protease inhibitors |
| EP1896032B1 (en) | 2005-06-14 | 2012-10-31 | Merck Sharp & Dohme Corp. | The preparation and use of compounds as protease inhibitors |
| TW200738683A (en) * | 2005-06-30 | 2007-10-16 | Wyeth Corp | Amino-5-(5-membered)heteroarylimidazolone compounds and the use thereof for β-secretase modulation |
| JP2009500329A (en) * | 2005-06-30 | 2009-01-08 | ワイス | Amino-5- (6 membered) heteroarylimidazolone compounds and their use for β-selectase modulation |
| TW200730523A (en) * | 2005-07-29 | 2007-08-16 | Wyeth Corp | Cycloalkyl amino-hydantoin compounds and use thereof for β-secretase modulation |
| AU2006294620A1 (en) * | 2005-09-26 | 2007-04-05 | Wyeth | Amino-5- [4- (difluoromethoxy) phenyl] -5-phenylimidazolone compounds as inhibitors of the beta-secretase (bace) |
| CN101346357B (en) | 2005-10-25 | 2014-04-02 | 盐野义制药株式会社 | Aminodihydrothiazine derivatives |
| JP2009520027A (en) * | 2005-12-19 | 2009-05-21 | ワイス | 2-Amino-5-piperidinylimidazolone compounds and their use in the regulation of β-secretase |
| WO2007100536A1 (en) * | 2006-02-24 | 2007-09-07 | Wyeth | DIHYDROSPIRO[DIBENZO[A,D][7]ANNULENE-5,4'-IMIDAZOL] COMPOUNDS FOR THE INHIBITION OF β-SECRETASE |
| US8168641B2 (en) | 2006-06-12 | 2012-05-01 | Schering Corporation | Aspartyl protease inhibitors |
| TW200815449A (en) * | 2006-06-14 | 2008-04-01 | Astrazeneca Ab | Novel compounds II |
| TW200815443A (en) * | 2006-06-14 | 2008-04-01 | Astrazeneca Ab | Novel compounds I |
| TW200808796A (en) * | 2006-06-14 | 2008-02-16 | Astrazeneca Ab | New compounds III |
| TW200815447A (en) * | 2006-06-14 | 2008-04-01 | Astrazeneca Ab | Novel compounds IV |
| TW200815349A (en) | 2006-06-22 | 2008-04-01 | Astrazeneca Ab | New compounds |
| US7700606B2 (en) * | 2006-08-17 | 2010-04-20 | Wyeth Llc | Imidazole amines as inhibitors of β-secretase |
| TW200817406A (en) * | 2006-08-17 | 2008-04-16 | Wyeth Corp | Imidazole amines as inhibitors of β-secretase |
| MX2009003102A (en) * | 2006-09-21 | 2009-04-01 | Wyeth Corp | Indolylalkylpyridin-2-amines for the inhibition of beta-secretase. |
| WO2008063114A1 (en) * | 2006-11-20 | 2008-05-29 | Astrazeneca Ab | Amino- imidazolones and their use as medicament for treating cognitive impairment alzheimer disease, neurodegeneration and dementia |
| MX2009006228A (en) | 2006-12-12 | 2009-06-22 | Schering Corp | Aspartyl protease inhibitors. |
| CL2008000784A1 (en) * | 2007-03-20 | 2008-05-30 | Wyeth Corp | AMINO-5 COMPOUNDS - [- 4- (DIFLOUROMETOXI) SUBSTITUTED PHENYL] -5-PHENYLMIDAZOLONE, B-SECRETASE INHIBITORS; PHARMACEUTICAL COMPOSITION THAT INCLUDES SUCH COMPOUNDS; AND ITS USE TO TREAT ALZHEIMER, COGNITIVE DETERIORATION, DOWN SYNDROME, DECREASE CO |
| PE20090617A1 (en) * | 2007-03-23 | 2009-05-08 | Wyeth Corp | AMINO-5 - [- 4- (DIFLUOROMETOXI) PHENYL] -5-PHENYLIMIDAZOLONE COMPOUNDS FOR THE INHIBITION OF -SECRETASE |
| JP5383483B2 (en) | 2007-04-24 | 2014-01-08 | 塩野義製薬株式会社 | Pharmaceutical composition for the treatment of Alzheimer's disease |
| EP2689780A1 (en) | 2007-04-24 | 2014-01-29 | Shionogi & Co., Ltd. | Intermediates for aminodihydrothiazine derivatives substituted with a cyclic group |
| TW200902499A (en) | 2007-05-15 | 2009-01-16 | Astrazeneca Ab | New compounds |
| AU2009239536C1 (en) | 2008-04-22 | 2012-12-13 | Merck Sharp & Dohme Corp. | Phenyl-substituted 2-imino-3-methyl pyrrolo pyrimidinone compounds as BACE-1 inhibitors, compositions, and their use |
| KR101324426B1 (en) | 2008-06-13 | 2013-10-31 | 시오노기세야쿠 가부시키가이샤 | SULFUR-CONTAINING HETEROCYCLIC DERIVATIVE HAVING β-SECRETASE-INHIBITING ACTIVITY |
| JP5417860B2 (en) * | 2008-08-26 | 2014-02-19 | 住友化学株式会社 | Method for producing α-hydroxyesters |
| US8426447B2 (en) | 2008-09-11 | 2013-04-23 | Amgen Inc. | Spiro-tricyclic ring compounds as beta-secretase modulators and methods of use |
| CN102186841A (en) | 2008-10-22 | 2011-09-14 | 盐野义制药株式会社 | 2-aminopyridin-4-one and 2-aminopyridine derivative both having bace1-inhibiting activity |
| TW201020244A (en) | 2008-11-14 | 2010-06-01 | Astrazeneca Ab | New compounds |
| EP2281824A1 (en) | 2009-08-07 | 2011-02-09 | Noscira, S.A. | Furan-imidazolone derivatives, for the treatment of cognitive, neurodegenerative or neuronal diseases or disorders |
| UA108363C2 (en) | 2009-10-08 | 2015-04-27 | IMINOTIADIASIADIOXIDE OXIDES AS BACE INHIBITORS, COMPOSITIONS THEREOF AND THEIR APPLICATIONS | |
| KR20120104570A (en) | 2009-12-11 | 2012-09-21 | 시오노기세야쿠 가부시키가이샤 | Oxazine derivative |
| US8883782B2 (en) | 2010-03-15 | 2014-11-11 | Amgen Inc. | Spiro-tetracyclic ring compounds as beta-secretase modulators and methods of use |
| JP5584352B2 (en) | 2010-03-15 | 2014-09-03 | アムジエン・インコーポレーテツド | Amino-dihydrooxazine and amino-dihydrothiazine spiro compounds as β-secretase modulators and their medical use |
| KR101730937B1 (en) | 2010-06-09 | 2017-04-27 | 얀센 파마슈티카 엔.브이. | 5,6-dihydro-2h-[1,4]oxazin-3-yl-amine derivatives useful as inhibitors of beta-secretase (bace) |
| EP2601197B1 (en) | 2010-08-05 | 2014-06-25 | Amgen Inc. | Amino-iso-indole, amino-aza-iso-indole, amino-dihydroisoquinoline and amino-benzoxazine compounds as beta-secretase modulators and methods of use |
| CN103261199A (en) | 2010-10-29 | 2013-08-21 | 盐野义制药株式会社 | Naphthyridine derivative |
| EP2634188A4 (en) * | 2010-10-29 | 2014-05-07 | Shionogi & Co | Fused aminodihydropyrimidine derivative |
| EP2643299B1 (en) | 2010-11-22 | 2016-06-22 | Noscira, S.A. | Bipyridine sulfonamide derivatives for the treatment of neurodegenerative diseases or conditions |
| EP2643325A1 (en) | 2010-11-23 | 2013-10-02 | Amgen Inc. | Spiro-amino-imidazolone and spiro-amino-dihydro-pyrimidinone compounds as beta-secretase modulators and methods of use |
| BR112013015430A2 (en) | 2010-12-22 | 2016-09-20 | Janssen Pharmaceutica Nv | 5,6-dihydroimidazo [1,2-a] pyrazin-8-ylamine derivatives useful as beta secretase (bace) inhibitors |
| US9346827B2 (en) | 2011-02-07 | 2016-05-24 | Amgen Inc. | 5-amino-oxazepine and 5-amino-thiazepane compounds as beta secretase antagonists and methods of use |
| US8962859B2 (en) | 2011-02-15 | 2015-02-24 | Amgen Inc. | Spiro-amino-imidazo-fused heterocyclic compounds as beta-secretase modulators and methods of use |
| CN103415519B (en) * | 2011-03-01 | 2016-03-02 | 詹森药业有限公司 | As 6,7-dihydro-pyrazol [1, the 5-a] pyrazine-4-yl amine derivatives that beta-secretase (BACE) inhibitor is useful |
| PH12013501805A1 (en) * | 2011-03-09 | 2013-11-18 | Janssen Pharmaceutica Nv | 3,4-DIHYDRO-PYRROLO[1,2-a]PYRAZIN-1-YLAMINE DERIVATIVES USEFUL AS INHIBITORS OF BETA-SECRETASE (BACE) |
| EP2694489B1 (en) | 2011-04-07 | 2017-09-06 | Merck Sharp & Dohme Corp. | C5-c6 oxacyclic-fused thiadiazine dioxide compounds as bace inhibitors, compositions, and their use |
| US9145426B2 (en) | 2011-04-07 | 2015-09-29 | Merck Sharp & Dohme Corp. | Pyrrolidine-fused thiadiazine dioxide compounds as BACE inhibitors, compositions, and their use |
| CN103608345A (en) | 2011-04-26 | 2014-02-26 | 盐野义制药株式会社 | Oxazine derivative and BACE 1 inhibitor containing same |
| US9181236B2 (en) | 2011-08-22 | 2015-11-10 | Merck Sharp & Dohme Corp. | 2-spiro-substituted iminothiazines and their mono-and dioxides as bace inhibitors, compositions and their use |
| JP2014526560A (en) | 2011-09-21 | 2014-10-06 | アムジエン・インコーポレーテツド | Aminooxazine and aminodihydrothiazine compounds as .BETA.-secretase modulators and methods of use |
| WO2014065434A1 (en) | 2012-10-24 | 2014-05-01 | Shionogi & Co., Ltd. | Dihydrooxazine or oxazepine derivatives having bace1 inhibitory activity |
| WO2014078314A1 (en) | 2012-11-15 | 2014-05-22 | Amgen Inc. | Amino-oxazine and amino-dihydrothiazine compounds as beta-secretase modulators and methods of use |
| US9751886B2 (en) | 2013-06-12 | 2017-09-05 | Janssen Pharmaceutica Nv | 4-amino-6-phenyl-6,7-dihydro[1,2,3]triazolo[1,5-A]pyrazine derivatives as inhibitors of beta-secretase (BACE) |
| WO2014198851A1 (en) | 2013-06-12 | 2014-12-18 | Janssen Pharmaceutica Nv | 4-amino-6-phenyl-5,6-dihydroimidazo[1,5-a]pyrazin-3(2h)-one derivatives as inhibitors of beta-secretase (bace) |
| CN105283457B (en) * | 2013-06-12 | 2018-09-18 | 詹森药业有限公司 | 4- amino -6- phenyl -5,6- glyoxalidine as beta-secretase (BACE) inhibitor simultaneously [1,5-A] pyrazines derivatives |
| CN105272960A (en) * | 2014-07-18 | 2016-01-27 | 上海科胜药物研发有限公司 | Preparation method of canagliflozin intermediate 2-(2-methyl-5-bromobenzyl)-5-(4-fluorobenzene)thiophene |
| ES2768823T3 (en) | 2014-12-18 | 2020-06-23 | Janssen Pharmaceutica Nv | 2,3,4,5-Tetrahydropyridin-6-amine and 3,4-dihydro-2H-pyrrole-5-amine derivatives useful as beta-secretase inhibitors |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IE45198B1 (en) | 1976-06-05 | 1982-07-14 | Wyeth John & Brother Ltd | Guanidine derivatives |
| DE2901362A1 (en) | 1978-01-25 | 1979-07-26 | Sandoz Ag | GUANIDE DERIVATIVES, THEIR PRODUCTION AND USE |
| GB1588096A (en) | 1978-05-20 | 1981-04-15 | Wyeth & Bros Ltd John | Pyrrole derivatives |
| GB9511694D0 (en) | 1995-06-09 | 1995-08-02 | Fujisawa Pharmaceutical Co | Benzamide derivatives |
| ZA967800B (en) | 1995-09-20 | 1997-04-03 | Yamanouchi Pharma Co Ltd | Heteroaryllsubstituted acryloylguanidine derivatives and pharmaceutical compositions comprising them |
| GB9611046D0 (en) | 1996-05-25 | 1996-07-31 | Wivenhoe Techn Ltd | Pharmacological compounds |
| GB2323841A (en) | 1997-04-04 | 1998-10-07 | Ferring Bv Group Holdings | Pyridine derivatives with anti-tumor and anti-inflammatory activity |
| TW544448B (en) | 1997-07-11 | 2003-08-01 | Novartis Ag | Pyridine derivatives |
| US6492408B1 (en) | 1999-07-21 | 2002-12-10 | Boehringer Ingelheim Pharmaceuticals, Inc. | Small molecules useful in the treatment of inflammatory disease |
| DE10024319A1 (en) | 2000-05-17 | 2001-11-22 | Merck Patent Gmbh | New bis-acylguanidine compounds are subtype-1 cellular sodium ion-proton antiporter inhibitors useful e.g. for treating arrhythmia, angina pectoris, infarction and insulin-independent diabetes mellitus |
| DE10046993A1 (en) | 2000-09-22 | 2002-04-11 | Aventis Pharma Gmbh | Substituted cinnamic acid guanidides, process for their preparation, their use as a medicament and medicament containing them |
| AU2002347022A1 (en) | 2001-12-20 | 2003-07-09 | Novo Nordisk A/S | Benzimidazols and indols as glucagon receptor antagonists/inverse agonisten |
| US7053220B2 (en) | 2002-02-01 | 2006-05-30 | Elan Pharmaceuticals, Inc. | Hydroxyalkanoyl aminopyrazoles and related compounds |
| WO2003094854A2 (en) * | 2002-05-07 | 2003-11-20 | Elan Pharmaceuticals, Inc. | Succinoyl aminopyrazoles and related compounds |
| GB0223038D0 (en) * | 2002-10-04 | 2002-11-13 | Merck Sharp & Dohme | Therapeutic compounds |
| AU2003299791A1 (en) | 2002-12-20 | 2004-07-22 | Bayer Pharmaceuticals Corporation | Substituted 3,5-dihydro-4h-imidazol-4-ones for the treatment of obesity |
| KR20060033873A (en) | 2003-07-01 | 2006-04-20 | 바이엘 크롭사이언스 게엠베하 | 3-pyridylcarboxamide derivatives as pesticides |
| US7700603B2 (en) | 2003-12-15 | 2010-04-20 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| SG163508A1 (en) | 2003-12-15 | 2010-08-30 | Schering Corp | Heterocyclic aspartyl protease inhibitors |
| US7592348B2 (en) | 2003-12-15 | 2009-09-22 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| ATE444962T1 (en) | 2004-06-16 | 2009-10-15 | Wyeth Corp | AMINO-5,5-DIPHENYLIMIDAZOLONE DERIVATIVES FOR BETA SECRETASE INHIBITION |
| JP2008503460A (en) * | 2004-06-16 | 2008-02-07 | ワイス | Diphenylimidazopyrimidine and imidazolamine as inhibitors of β-secretase |
| BRPI0607094A2 (en) | 2005-02-01 | 2009-08-04 | Wyeth Corp | compound of the formula i; use of the compound for the treatment of a disease or disorder associated with excessive baby activity in a patient who needs it; use of the compound to modulate the bace activity; and pharmaceutical composition |
| WO2006088694A1 (en) | 2005-02-14 | 2006-08-24 | Wyeth | SUBSTITUTED THIENYL AND FURYL ACYLGUANIDINES AS β-SECRETASE MODULATORS |
| CN101146769A (en) | 2005-02-14 | 2008-03-19 | 惠氏公司 | Azolylacylguanidines as β-secretase inhibitors |
| WO2006088705A1 (en) | 2005-02-14 | 2006-08-24 | Wyeth | Terphenyl guanidines as [beta symbol] -secretase inhibitors |
| JP2009500329A (en) | 2005-06-30 | 2009-01-08 | ワイス | Amino-5- (6 membered) heteroarylimidazolone compounds and their use for β-selectase modulation |
| TW200738683A (en) | 2005-06-30 | 2007-10-16 | Wyeth Corp | Amino-5-(5-membered)heteroarylimidazolone compounds and the use thereof for β-secretase modulation |
| TW200730523A (en) | 2005-07-29 | 2007-08-16 | Wyeth Corp | Cycloalkyl amino-hydantoin compounds and use thereof for β-secretase modulation |
| AU2006294620A1 (en) | 2005-09-26 | 2007-04-05 | Wyeth | Amino-5- [4- (difluoromethoxy) phenyl] -5-phenylimidazolone compounds as inhibitors of the beta-secretase (bace) |
| JP2009520027A (en) | 2005-12-19 | 2009-05-21 | ワイス | 2-Amino-5-piperidinylimidazolone compounds and their use in the regulation of β-secretase |
| WO2007100536A1 (en) | 2006-02-24 | 2007-09-07 | Wyeth | DIHYDROSPIRO[DIBENZO[A,D][7]ANNULENE-5,4'-IMIDAZOL] COMPOUNDS FOR THE INHIBITION OF β-SECRETASE |
| US7700606B2 (en) | 2006-08-17 | 2010-04-20 | Wyeth Llc | Imidazole amines as inhibitors of β-secretase |
-
2006
- 2006-01-09 EP EP10173563A patent/EP2264036A1/en not_active Withdrawn
- 2006-01-09 CN CNA2006800021783A patent/CN101103034A/en active Pending
- 2006-01-09 JP JP2007551307A patent/JP2008526966A/en not_active Withdrawn
- 2006-01-09 MX MX2007008555A patent/MX2007008555A/en unknown
- 2006-01-09 BR BRPI0606690-9A patent/BRPI0606690A2/en not_active IP Right Cessation
- 2006-01-09 AU AU2006205127A patent/AU2006205127A1/en not_active Abandoned
- 2006-01-09 WO PCT/US2006/000656 patent/WO2006076284A2/en not_active Ceased
- 2006-01-09 EP EP06717815A patent/EP1836208A2/en not_active Withdrawn
- 2006-01-09 RU RU2007126570/04A patent/RU2007126570A/en unknown
- 2006-01-09 CA CA002593515A patent/CA2593515A1/en not_active Abandoned
- 2006-01-09 KR KR1020077016053A patent/KR20070095948A/en not_active Withdrawn
- 2006-01-10 PE PE2006000052A patent/PE20060842A1/en not_active Application Discontinuation
- 2006-01-11 GT GT200600009A patent/GT200600009A/en unknown
- 2006-01-13 AR ARP060100150A patent/AR052458A1/en not_active Application Discontinuation
- 2006-01-13 PA PA20068660001A patent/PA8660001A1/en unknown
- 2006-01-13 US US11/332,732 patent/US7563796B2/en not_active Expired - Fee Related
- 2006-01-13 TW TW095101509A patent/TW200637866A/en unknown
-
2007
- 2007-06-14 IL IL183938A patent/IL183938A0/en unknown
- 2007-06-18 NO NO20073099A patent/NO20073099L/en not_active Application Discontinuation
- 2007-07-12 CR CR9244A patent/CR9244A/en not_active Application Discontinuation
- 2007-07-13 ZA ZA200705783A patent/ZA200705783B/en unknown
-
2009
- 2009-06-18 US US12/487,395 patent/US20090253716A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20090253716A1 (en) | 2009-10-08 |
| WO2006076284A2 (en) | 2006-07-20 |
| CN101103034A (en) | 2008-01-09 |
| IL183938A0 (en) | 2007-10-31 |
| WO2006076284A3 (en) | 2007-04-19 |
| TW200637866A (en) | 2006-11-01 |
| ZA200705783B (en) | 2008-09-25 |
| BRPI0606690A2 (en) | 2009-07-14 |
| AU2006205127A1 (en) | 2006-07-20 |
| JP2008526966A (en) | 2008-07-24 |
| RU2007126570A (en) | 2009-02-20 |
| CA2593515A1 (en) | 2006-07-20 |
| PE20060842A1 (en) | 2006-10-12 |
| KR20070095948A (en) | 2007-10-01 |
| US20060160828A1 (en) | 2006-07-20 |
| NO20073099L (en) | 2007-07-31 |
| PA8660001A1 (en) | 2006-09-08 |
| US7563796B2 (en) | 2009-07-21 |
| GT200600009A (en) | 2006-08-17 |
| EP1836208A2 (en) | 2007-09-26 |
| EP2264036A1 (en) | 2010-12-22 |
| AR052458A1 (en) | 2007-03-21 |
| MX2007008555A (en) | 2007-11-21 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal (granting procedure) |